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Published on: May 4, 2021
ANGPTL4 silencing via antisense oligonucleotides reduces plasma triglycerides and glucose in mice without causing
Mingjuan Deng1, Elda Kutrolli2, Anne Sadewasser3
1Nutrition, Metabolism and Genomics Group, Division of Human Nutrition and Health, Wageningen University, Wageningen, the Netherlands.
Abstract:
Angiopoietin-like 4 (ANGPTL4) is an important regulator of plasma triglyceride (TG) levels and an attractive pharmacological target for lowering plasma lipids and reducing cardiovascular risk. Here, we aimed to study the efficacy and safety of silencing ANGPTL4 in the livers of mice using hepatocyte-targeting GalNAc-conjugated antisense oligonucleotides (ASOs). Compared with injections with negative control ASO, four injections of two different doses of ANGPTL4 ASO over 2 weeks markedly downregulated ANGPTL4 levels in liver and adipose tissue, which was associated with significantly higher adipose LPL activity and lower plasma TGs in fed and fasted mice, as well as lower plasma glucose levels in fed mice. In separate experiments, injection of two different doses of ANGPTL4 ASO over 20 weeks of high-fat feeding reduced hepatic and adipose ANGPTL4 levels but did not trigger mesenteric lymphadenopathy, an acute phase response, chylous ascites, or any other pathological phenotypes. Compared with mice injected with negative control ASO, mice injected with ANGPTL4 ASO showed reduced food intake, reduced weight gain, and improved glucose tolerance. In addition, they exhibited lower plasma TGs, total cholesterol, LDL-C, glucose, serum amyloid A, and liver TG levels. By contrast, no significant difference in plasma alanine aminotransferase activity was observed. Overall, these data suggest that ASOs targeting ANGPTL4 effectively reduce plasma TG levels in mice without raising major safety concerns.
Insights
Silencing Angiopoietin-like 4 (ANGPTL4) with antisense oligonucleotides (ASOs) in mice effectively lowered plasma triglycerides and improved glucose metabolism. This ANGPTL4 ASO treatment demonstrated a favorable safety profile in preclinical studies.
Area of Science:
- Biochemistry
- Pharmacology
- Genetics
Background:
- Angiopoietin-like 4 (ANGPTL4) is a key regulator of plasma triglyceride (TG) levels.
- ANGPTL4 is a potential pharmacological target for managing dyslipidemia and cardiovascular disease.
- Antisense oligonucleotides (ASOs) offer a method for gene silencing.
Purpose of the Study:
- To investigate the efficacy of hepatocyte-targeting GalNAc-conjugated ASOs in silencing ANGPTL4 in mice.
- To assess the impact of ANGPTL4 silencing on plasma lipid levels, glucose metabolism, and safety.
Main Methods:
- Mice received ANGPTL4-targeting ASOs or control ASOs via injections.
- Studies included short-term (2 weeks) and long-term (20 weeks) high-fat feeding protocols.
- Measurements included ANGPTL4 levels, adipose LPL activity, plasma lipids, glucose, body weight, and safety markers.
Main Results:
- ANGPTL4 ASOs significantly downregulated ANGPTL4 in liver and adipose tissue, increasing LPL activity and reducing plasma TGs.
- Long-term treatment improved glucose tolerance, reduced food intake, and decreased weight gain.
- No significant adverse effects such as lymphadenopathy or ascites were observed; liver enzymes remained normal.
Conclusions:
- Hepatocyte-targeted ANGPTL4 ASOs are effective in reducing plasma TG levels in mice.
- This therapeutic strategy shows a promising safety profile, suggesting potential for cardiovascular risk reduction.
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